CAMPYLOBACTER AGAR BASE
K-Number: K840332 · 1984-05-11
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Device Summary
Frequently Asked Questions
What is the CAMPYLOBACTER AGAR BASE?
CAMPYLOBACTER AGAR BASE is a medical device that received FDA 510(k) clearance on 1984-05-11. The listed applicant is Oxoid U.S.A., Inc.. The 510(k) number is K840332.
When did CAMPYLOBACTER AGAR BASE receive FDA 510(k) clearance?
CAMPYLOBACTER AGAR BASE received FDA 510(k) clearance on 1984-05-11, under 510(k) number K840332.
Who is the listed applicant for CAMPYLOBACTER AGAR BASE?
The FDA 510(k) record lists Oxoid U.S.A., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CAMPYLOBACTER AGAR BASE?
The FDA product code for CAMPYLOBACTER AGAR BASE is JSJ.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Oxoid U.S.A., Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: JSJ)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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